• Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

510(k) Premarket Notification

  • Print
  • Share
  • E-mail
-
Super Search Devices@FDA
510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
CFR Title 21 | Radiation-Emitting Products | X-Ray Assembler | Medsun Reports | CLIA | TPLC
 


New Search Back To Search Results
Device Classification Name biuret (colorimetric), total protein
510(k) Number K950128
Device Name TOTAL PROTEIN TEST (TPRO) ITEM XXXXX/R1. R2
Applicant
EMD CHEMICALS INC.
DIV. OF EM INDUSTRIES INC.
480 DEMOCRAT RD.
GIBBSTOWN,  NJ  08027
Applicant Contact CAROL FAULKNER
Correspondent
EMD CHEMICALS INC.
DIV. OF EM INDUSTRIES INC.
480 DEMOCRAT RD.
GIBBSTOWN,  NJ  08027
Correspondent Contact CAROL FAULKNER
Regulation Number862.1635
Classification Product Code
CEK  
Date Received01/12/1995
Decision Date 05/15/1995
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Clinical Chemistry
510k Review Panel Clinical Chemistry
Type Traditional
Reviewed by Third Party No
Combination Product No
-
-